Cloning, Sequencing and Analyzing of 16S rRNA Gene from Inulin Hydrolyzing Bacteria

Authors

  • Ahadul Putra Faculty of Mathematics and Natural Science, Universitas Negeri Padang, Indonesia
  • Minda Azhar Faculty of Mathematics and Natural Science, Universitas Negeri Padang, Indonesia
  • Iryani Faculty of Mathematics and Natural Science, Universitas Negeri Padang, Indonesia
  • Yuni Ahda Faculty of Mathematics and Natural Science, Universitas Negeri Padang, Indonesia
  • Fernita Puspasari Faculty of Mathematics an Natural Science, Institut Teknologi Bandung, Indonesia
  • Ihsanawati Faculty of Mathematics an Natural Science, Institut Teknologi Bandung, Indonesia
  • Dessy Natalia Faculty of Mathematics an Natural Science, Institute of Technology Bandung, Indonesia

DOI:

https://doi.org/10.31695/IJASRE.2020.33790

Keywords:

Inulin Hydrolyzing Bacteria, 16S Rrna Gene, Pgem-T Easy, Inulin.

Abstract

Gene of 16S rRNA is used for molecular identification of bacteria. This research aims to analyze the sequences of 16S rRNA gene from inulin hydrolyzing bacteria of UKG isolate. The 16S rRNA gene was isolated by PCR using BacF1 and UniB1 primers. The gene was cloned to pGEM-T Easy vector with E.coli TOP10F as host cell. Recombinant DNA was sequenced using T7 and SP6 primers. The size of the nucleotide base of the recombinant DNA of the sequencing result using SP6 primer was 1167 bp, whereas using T7 primer was 1218 bp. The both of the sequences overlapped 760 bp. The size of 16S rRNA gene in the sequences was found 1501 bp. Recombinant DNA that was restricted using EcoR1 showed 3 bands on agarose gel. They were 3000 bp, 800 bp, and 700 bp. The position of the EcoR1 palindrome sequence on the 16S rRNA gene was at the 832-837. The 16S rRNA gene also has been known by HindIII, BamHI, BalI, HaeIII, and SmaI restriction enzymes.

References

Sirisansaneeyakul S. Worawuthiyanan N, Vanichsriratana W, Srinophakun P, Chisti Y. 2007. Production of Fructose from Inulin Using Mixed Inulinases from Aspergillus niger and Candida guilliermondii. World J Microbiol Biotechnol.DOI 10.1007/s11274-006-9258-6.

Chi, M.Z. 2011. Biotechnological Potential of Inulin for Bioprocesses. Bioresource Technology 102 (2011) 4295–4303. doi: 10.1016/j. biotech.2010.12. 086.

Zittan, L.1981. Enzymatic Hydrolysis of Inulin an Alternative Way to Fructose Production. Starch,33:373-377.

Ozturk, B., & Serdaroğlu.M. 2017. A Rising Star Prebiotic Dietary Fiber: Inulin and Recent Applications in Meat Products. Journal of food and health science 3(1): 12-20 (2017) doi: 10.3153/JFHS17002.

Singh, R.S.,Chauhan, K., dan John F. Kennedy. 2017. a Panorama of Bacterial Inulinases: Production, Purification, Characterization and Industrial Applications. International Journal of Biological Macromolecules 96(2017) 312322 .http ://dx.doi.org/10.1016/j.ijbiomac. 2017.12.004.

Ntushelo, Khayalethu. 2013. Identifying Bacteria and Studying Bacterial Diversity Using the 16S Ribosomal RNA gene-based Sequencing Techniques: A review. Afr. J. Microbiol. Res. DOI:10.5897/ ajmr 2013.5966.

Jenkins C, Ling CL, Ciesielczuk HL, Lockwood J, Hopkins S, McHugh TD, Gillespie SH, Kibbler CC. 2012. Detection and Identification of Bacteria in Clinical Samples by 16S rRNA Gene Sequencing: Comparison of Two Different Approaches in Clinical Practice. Journal of Medical Microbiology (2012), 61, 483–488. DOI 10.1099/jmm.0.030387.

Smith, D.A & Baker, J.J. Cowan.2003. Review and Re-analysis of Domain Specific 16S rRNA Primers. Journal of Microbiological Methods 55 (2003) 541–555.doi:10.1016/j.mimet. 2003. 08.009.

Janda, Michael and Abbott, L Sharon. 2007. 16S rRNA Gene Sequencing for Bacterial Identification in the Diagnostic Laboratory: Pluses, Perils, and Pitfalls. J. Clin. Microbiol. 2007, 45(9):2761. DOI: 10.1128/JCM.01228-07.

Weisburg WG1, Barns SM, Pelletier DA, Lane DJ. 1991. 16S Ribosomal DNA Amplification for Phylogenetic Study.

Journal of Bacteriology, Jan. 1991, p. 697-703 Vol. 173, No. 2.

Azhar, M.,Dessy Natalia., Sumaryati Syukur, Vovien and Jamsari. 2015. Gene Fragments that Encodes Inulin Hydrolysis Enzyme from Genomic Bacillus licheniformis: Isolation by PCR Technique Using New Primers. International Journal of Biological Chemistry 9 (2): 59-69, 2015. DOI: 10.3923/ijbc.2015.59. 69.

Castro, G.R., M.D. Baigori and F.Sineriz, 1995. A Plate Technique for Screening of Inulin Degrading Microorganisms. J. Microbiol. Meth., 22: 51-56.

Sambrook, J., E.F. Fritish and T. Maniatis, 1989. Molecular Cloning: A Laboratory Manual. 2nd Edn., Cold Spring Harbor Laboratory Press, New York, USA., ISBN-13: 978-0879693091.

Azhar, M., Ahda, Y., Ihsanawati, Puspasari, F., Mawarni, S.,Risa, B., Natalia, D. 2017.Skrining Bakteri Penghidrolisis Inulin dari Rizosfer Umbi Dahlia Menggunakan Inulin Umbi Dahlia. Eksakta Vol. 18 No. 2. E-ISSN : 2549-7464, P-ISSN : 1411-3724.

www.Promega.com .Wizard® Genomic DNA Purification Kit. Accessed November 25th, 2018.

Nelson, L.D., & Michael. 2012. Principles of Biochemistry Sixth Edition.New York: United States of America.

Magdeldin, Sameh.2012. Gel Electrophoresis – Principles and Basic. Croatia:InTech.

Smith, R.H., Willshaw, A. 1979. Application of Agarose Gel Electrophoresis to the Characterization of Plasmid DNA in Drug-resistant Enterobacteria. Journal of General Microbiology (1979), 114, 15-25.

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How to Cite

Ahadul Putra, Minda Azhar, Iryani, Yuni Ahda, Fernita Puspasari, Ihsanawati, & Dessy Natalia. (2020). Cloning, Sequencing and Analyzing of 16S rRNA Gene from Inulin Hydrolyzing Bacteria . International Journal of Advances in Scientific Research and Engineering (IJASRE), ISSN:2454-8006, DOI: 10.31695/IJASRE, 6(5), 88–95. https://doi.org/10.31695/IJASRE.2020.33790

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